Taiwan FDA registration 9da29fd2335f240c738ed7a0dd3724e1

"Rexxam" Digital Visual Acuity Chart (Non-Sterile)

TW: "隆祥" 視力檢查儀(未滅菌)

Taiwan·Risk Class 1·MD·REXXAM CO., LTD. KAGAWA FACTORY·Registered May 18, 2020 – May 18, 2025Expired

Registration details

Analysis ID: 9da29fd2335f240c738ed7a0dd3724e1
License Form: Ministry of Health Medical Device Import No. 021545
Customs Code: DHA09402154506

Company information

Manufacturer: REXXAM CO., LTD. KAGAWA FACTORY
Manufacturer Country: Japan
Authorized Representative: TAIWAN INSTRUMENT CO., LTD.

Product details

Intended Use: Limited to the first level recognition range of ophthalmic projectors (M.1680) for the management of medical equipment.
Product Type (Level 1): M Ophthalmic devices
Product Type (Level 2): M1680 Ophthalmic Projector
Import Information: Imported from abroad

Dates and status

Registration Date: May 18, 2020
Expiry Date: May 18, 2025

About this record

Access comprehensive regulatory information for "Rexxam" Digital Visual Acuity Chart (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9da29fd2335f240c738ed7a0dd3724e1 and manufactured by REXXAM CO., LTD. KAGAWA FACTORY. The authorized representative in Taiwan is TAIWAN INSTRUMENT CO., LTD..

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